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Local structure tuning in Fe-N-C catalysts through support effect for boosting CO2 electroreduction
[Display omitted] •Preparation of a single-atom catalyst by coordination strategy.•Tuning local electronic and geometric structure of active sites by changing carbon support.•Higher Faradaic efficiency of CO at −0.5 V vs. RHE.•DFT calculations demonstrate axial Fe-N coordination has excellent perfor...
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Published in: | Applied catalysis. B, Environmental Environmental, 2020-09, Vol.272, p.118960, Article 118960 |
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Main Authors: | , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | [Display omitted]
•Preparation of a single-atom catalyst by coordination strategy.•Tuning local electronic and geometric structure of active sites by changing carbon support.•Higher Faradaic efficiency of CO at −0.5 V vs. RHE.•DFT calculations demonstrate axial Fe-N coordination has excellent performance for CO2RR.
Metal-N-C materials have attracted considerable attention for electrocatalytic CO2 reduction. Local electronic and geometric structure of active sites in the metal-N-C catalysts significantly determine catalytic reactivity. In this work, atomically dispersed Fe species with different coordination environment are anchored into carbon supports through introducing aminated carbon nanotubes, as effectively revealed by the Cs-corrected transmission electron microscope and X-ray absorption near edge structure spectra. Electrochemical tests show that the catalyst with the aminated carbon nanotubes has a low overpotential (0.39 V) and high selectivity of CO up to 95.47 % at -0.6 V vs. RHE. The density functional theory calculation results indicate that the additional axial Fe-N coordination compared with the planar Fe-N coordination can reduce the free energy required for the desorption of CO from the adsorption site and inhibit the occurrence of hydrogen evolution reaction, thus leading to improve the selectivity of CO. |
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ISSN: | 0926-3373 1873-3883 |
DOI: | 10.1016/j.apcatb.2020.118960 |